JP5296957B2 - Anti-aging agent for oral use - Google Patents

Anti-aging agent for oral use Download PDF

Info

Publication number
JP5296957B2
JP5296957B2 JP2004066262A JP2004066262A JP5296957B2 JP 5296957 B2 JP5296957 B2 JP 5296957B2 JP 2004066262 A JP2004066262 A JP 2004066262A JP 2004066262 A JP2004066262 A JP 2004066262A JP 5296957 B2 JP5296957 B2 JP 5296957B2
Authority
JP
Japan
Prior art keywords
aging
rice
present
product
added
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP2004066262A
Other languages
Japanese (ja)
Other versions
JP2005255557A (en
Inventor
孝 徳山
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Soken Co Ltd
Original Assignee
Soken Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Soken Co Ltd filed Critical Soken Co Ltd
Priority to JP2004066262A priority Critical patent/JP5296957B2/en
Publication of JP2005255557A publication Critical patent/JP2005255557A/en
Application granted granted Critical
Publication of JP5296957B2 publication Critical patent/JP5296957B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Landscapes

  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Medicines Containing Plant Substances (AREA)

Description

本発明は、米由来成分を有効成分とする、経口用老化防止剤に関するものである。   The present invention relates to an oral antiaging agent containing a rice-derived component as an active ingredient.

人は誰しも年を取るにつれて老化現象が現れ、やがて死を迎えるという現実からは逃れることはできない。しかし老化を防ぐことができれば、死を迎える間際まで健康に過ごすことは可能である。老化とは歳をとるにつれ身体の機能が衰えることである。即ち、加齢とともに各臓器の機能や臓器間の統合機能が低下し身体の恒常性を維持し得なくなる現象である。老化の原因はいくつかの説が提唱されており、例えば、染色体の両末端にあるテロメアの短小化により細胞分裂が停止し、老化を引き起こすとするテロメア説や、細胞分裂のプロセスで起こった複製エラーによりできたエラー蛋白質が蓄積することによるというエラー説など遺伝子レベルでの老化説のほか、活性酸素がDNAや蛋白質、細胞膜などの脂質を攻撃し老化を引き起こすという活性酸素説などがある。   No one can escape from the reality that aging appears as people age and eventually dies. However, if we can prevent aging, we can stay healthy until just before death. Aging means that the function of the body declines with age. That is, it is a phenomenon in which the function of each organ and the integration function between organs decrease with aging, and the homeostasis cannot be maintained. Several theories have been proposed for the cause of aging, for example, the telomere theory that cell division stops due to shortening of telomeres at both ends of the chromosome and causes aging, and replication that occurred in the process of cell division In addition to the aging theory at the gene level, such as the error theory that error proteins are caused by error accumulation, there is the reactive oxygen theory that active oxygen attacks lipids such as DNA, proteins, and cell membranes to cause aging.

また老化防止のために検討されている手段としては、遺伝子を操作して加齢による影響を食い止める、テロメラーゼ遺伝子を導入することにより無限増殖を可能にする、活性酸素抑制酵素を生成する遺伝子を活性化させるといった遺伝子操作や、抗酸化物質やSOD様活性物質の補給による活性酸素消去などがある。しかし、遺伝子操作、遺伝子組み換えによる方法は安全性に問題があり、また老化は様々な要因がからみあってもたらされるため、特定の要因に着目した方法では個体レベルで効果を発現させるのは困難である。
WO01/088149 特許公表2003―508079
In addition, as a means studied to prevent aging, the gene is manipulated to stop the effects of aging, the telomerase gene is introduced to enable infinite growth, and the gene that generates reactive oxygen suppression enzyme is activated. There are gene manipulation such as oxidization and elimination of active oxygen by supplementation with antioxidants and SOD-like active substances. However, genetic engineering and genetic recombination methods have safety problems, and aging is entangled with various factors, so it is difficult to achieve effects at the individual level with methods that focus on specific factors. .
WO01 / 088149 Patent publication 2003-508079

個体は細胞により構成されていることから、細胞レベルでの老化が結果として個体の老化へとつながる。そこで本発明は、遺伝子操作を行うことなくまた、抗酸化物質やSOD様活性物質の補給による活性酸素消去作用によることなく、細胞の老化を防止しさらには細胞により構成される組織や臓器、器官、個体の老化を防止する有効な新規成分の提供を目的とする。   Since an individual is composed of cells, aging at the cellular level results in aging of the individual. Therefore, the present invention prevents cells from aging without performing genetic manipulation, and without eliminating the active oxygen by supplementing antioxidant substances or SOD-like active substances, and further, tissues, organs, organs composed of cells An object of the present invention is to provide an effective new ingredient for preventing aging of an individual.

本発明者らは、動植物和すの観点から、主食である米を中心に種々の植物成分の研究を進めてきた。その過程で、米は今まで予測できなかった数多くの可能性及び効果があることが判明してきた。そこで、主食として用いられ、安全性が最も高いことが実証されている米をテーマとして取り上げ、米の総合利用研究を行ってきた。そのうちの一つのテーマとして、老化防止について鋭意研究を重ねてきたのであるが、その過程で米には経口摂取により老化防止効果を発揮する成分が含有されていることを見出し、本発明を完成するに至った。   The inventors of the present invention have been researching various plant components, mainly rice, which is a staple food, from the viewpoint of fauna and flora. In the process, rice has been found to have many possibilities and benefits that could not have been predicted before. Therefore, we have taken up the theme of rice, which is used as a staple food and has proven to be the safest, and has conducted comprehensive rice research. As one of the themes, we have conducted intensive research on aging prevention. In the process, we have found that rice contains ingredients that exhibit anti-aging effects when taken orally, and complete the present invention. It came to.

本発明において、米由来のどのような成分(又は複数の成分の組合わせ、或いは所定存在比での複数の成分の組合わせ)が老化防止効果を有するのかに関しては、未だ解明するに至ってないが、米を原料として所定の処理を施したものを、経口的に摂取することにより、生命体或いは個体、器官、臓器、組織、体液又は細胞、遺伝子機能などの老化防止効果を示すことが判明した。また、本発明に係る老化防止剤が、老化防止、老化改善、若さ保持、若返り作用をもつことも判明した。なお、老化防止効果の作用機序は明らかではないが、活性酸素消去作用、SOD様活性によらない、非SOD様活性型の作用であると考えられる。   In the present invention, it has not yet been elucidated as to what component derived from rice (or a combination of a plurality of components or a combination of a plurality of components at a predetermined abundance ratio) has an anti-aging effect. It has been found that, when orally ingested using rice as a raw material, it exhibits anti-aging effects on living organisms or individuals, organs, organs, tissues, body fluids or cells, gene functions, etc. . It has also been found that the anti-aging agent according to the present invention has anti-aging, aging improvement, youth retention and rejuvenation actions. Although the mechanism of action of the anti-aging effect is not clear, it is considered that it is a non-SOD-like active action that does not depend on the active oxygen scavenging action or SOD-like activity.

即ち、本発明(1)は、米の粉砕物を有効成分として含有する経口用老化防止剤である。   That is, the present invention (1) is an antiaging agent for oral use containing pulverized rice as an active ingredient.

本発明(2)は、米の抽出物を有効成分として含有する経口用老化防止剤である。   The present invention (2) is an oral antiaging agent containing rice extract as an active ingredient.

本発明(3)は、米の加水物を酵素分解または麹を作用させたものを有効成分として含有する経口用老化防止剤である。   The present invention (3) is an antiaging agent for oral use containing, as an active ingredient, a rice hydrolyzate that has been subjected to enzymatic degradation or koji action.

本発明(4)は、米を抽出するに当たり、その抽出前、抽出と同時または抽出後に酵素分解または麹を作用させたものを有効成分として含有する経口用老化防止剤である。   The present invention (4) is an antiaging agent for oral use containing, as an active ingredient, an enzyme that has been subjected to enzymatic degradation or koji before, during or after extraction of rice.

本発明(5)は、米の抽出物あるいは酵素分解または麹を作用させたものに、アルコール発酵あるいは有機酸発酵を行ったものを有効成分として含有する経口用老化防止剤である。   The present invention (5) is an antiaging agent for oral use containing, as an active ingredient, a product obtained by subjecting an extract of rice or enzymatic degradation or koji to alcohol fermentation or organic acid fermentation.

本発明によれば、生命体或いは個体、器官、臓器、組織、体液又は細胞の老化防止、老化改善、若々しさ保持、若返りができる。従って、老化皮膚、老人性乾皮症、皮膚老化症状(しわ、ハリ・弾力の低下、たるみ、シミ、色の変化、乾燥)、記憶力低下、学習能力の低下、筋力の衰え、体力低下、内分泌系の機能の低下、視力の低下、聴力の低下、反射神経が鈍くなる、外からの刺激に対する反応が遅くなる、外からの刺激により起こった体の中の変化がもとの状態に戻るまでに時間がかかる、傷の治りが悪くなる、免疫機能の低下、ウイルス、細菌に対する抵抗力が衰えるなど生理機能の低下に対する予防、改善効果をもつものである。また、老化により発症する各種疾患の予防、改善効果ももつものである。   According to the present invention, it is possible to prevent aging, improve aging, maintain youthfulness, and rejuvenate living organisms or individuals, organs, organs, tissues, body fluids or cells. Therefore, aging skin, senile xeroderma, skin aging symptoms (wrinkles, reduced elasticity, sagging, blemishes, color change, dryness), decreased memory, learning ability, muscle weakness, weakness, endocrine Decline in system function, visual acuity, hearing loss, dull reflexes, slow response to external stimuli, until changes in the body caused by external stimuli return to their original state It has the effect of preventing and improving the deterioration of physiological functions such as taking time, worsening the healing of wounds, decreasing immune function, and decreasing resistance to viruses and bacteria. It also has the effect of preventing and improving various diseases that develop due to aging.

また、米は、今まで主食であったため、新規な利用用途はほとんど開発されていなかった。さらには、米は今まで主食とされてきたものであり、安全性も実証されているものである。すなわち、本発明は、非常に優れた経口用老化防止効果を持っているばかりでなく、安全性も十分に実証されているものを見出したものであり、さまざまな医薬品、医薬部外品、健康食品、飲食品に利用できる非常に有意義な発明といえる。また、米の過剰生産といわれている現在、新たな米の利用用途を見出したこと、および米のイメージアップによる消費拡大を図りうることは、極めて有意義なことである。   In addition, rice has been a staple food so far, and new uses have hardly been developed. In addition, rice has been a staple food and has been proven to be safe. That is, the present invention has been found not only to have an excellent anti-aging effect for oral aging, but also has been well-proven safety, various drugs, quasi drugs, health It can be said that it is a very significant invention that can be used for foods and foods. In addition, it is extremely meaningful that we have found new uses for rice and are able to expand consumption by improving the image of rice.

本発明に係る「米」とは、白米、玄米及び発芽させた米といった米だけでなく、白糠及び赤糠等といった米の一部も含む概念である。但し、白米部分を必須的に含むもの、即ち、白米、玄米、発芽させた米、白糠を用いることが好適である。ここで、白米及び玄米に関しては、ジャポニカ、インディカ米を問わず、うるち米、および餅米等の玄米および白米を指し、品種、種類は問わない。また、白糠及び赤糠とは、一般に、精白時に出てくる92%以上の赤糠や92%以下の白糠を指すが、両者が混合したものを使用してもよい。なお、有効成分は、熱および光に対して安定であるため、上記の原料は、浸漬、蒸煮、焙煎(砂焙り、網焙り、熱風焙煎等全てを指す)、蒸煮焙煎、凍結乾燥等の表面変性、UV照射等の光変性、パットライス等の加圧焙煎、揚げる等の原料処理をしてもよい。白米、玄米及び発芽させた米は、そのまま用いても有効であるが、実用上の面から粉砕して用いるのが好ましい。白米、玄米及び発芽させた米を粉砕して粉体化するには、粉砕機または精米機を用い一般的な方法で行なえばよい。   “Rice” according to the present invention is a concept that includes not only rice such as white rice, brown rice and germinated rice, but also part of rice such as white rice and red rice bran. However, it is preferable to use one that essentially contains a white rice portion, that is, white rice, brown rice, germinated rice, or white birch. Here, with respect to white rice and brown rice, it refers to brown rice and white rice such as glutinous rice and glutinous rice regardless of japonica and indica rice. In addition, white rabbit and red rabbit generally refer to 92% or more red rabbit or 92% or less white rabbit that appears at the time of whitening, but a mixture of both may be used. In addition, since the active ingredient is stable to heat and light, the above-mentioned raw materials are dipping, steaming, roasting (pointing to all of sand roasting, net roasting, hot air roasting, etc.), steaming roasting, freeze drying It may be subjected to raw material treatment such as surface modification such as UV irradiation, photo-modification such as UV irradiation, pressure roasting such as Patrice, frying. White rice, brown rice, and germinated rice are effective when used as they are, but are preferably pulverized for practical use. In order to pulverize white rice, brown rice and germinated rice into powder, a general method may be used using a pulverizer or a rice mill.

発芽させた米を製造する場合、胚芽のついた米を水に浸漬あるいは水を噴霧して発芽させる。発芽させる時の温度は5〜70℃である。ただし、発芽さえすれば、温度および時間は問わない。また、発芽中に水が腐敗する危険性がある場合は、腐敗しないように水を取り替えるか、何らかの防腐を行うのが好ましい。ここで、発芽とは、発芽する直前から発芽したものまで全てを指す。この発芽させた米をよく洗浄して用いる。この時、乾燥して用いてもよい。米を抽出、あるいは酵素分解または麹を作用させる場合、原料の米を粉砕して顆粒あるいは粉体化すると、表面積が大きくなるため効率がよくなる。粉砕しなくてもよいが、この場合には、米組織の分解および抽出に長時間を要する。   In the case of producing germinated rice, germinated rice is immersed in water or sprayed with water. The temperature at the time of germination is 5-70 degreeC. However, the temperature and time are not limited as long as germination occurs. In addition, when there is a risk of water rot during germination, it is preferable to replace the water so that it does not rot or to perform some preservative. Here, germination refers to everything from just before germination to germination. The germinated rice is washed thoroughly before use. At this time, you may dry and use. When rice is extracted, or enzymatically decomposed or subjected to koji, the raw material rice is pulverized into granules or powders, so that the surface area is increased and the efficiency is improved. Although it is not necessary to grind, in this case, it takes a long time to decompose and extract the rice tissue.

米を水抽出する場合、抽出温度は、高温が効率的であるが、低温でも十分に抽出を行うことができる。ただし、40℃以下の低温の場合は、pHを酸性あるいはアルカリ性にするか、防腐剤あるいはアルコールを加えて、米が腐敗しないように処理することが望ましい。抽出時間は、有効成分さえ抽出できれば、長くても短くてもよく、抽出温度により定めればよい。また、抽出は、加圧下または常圧下で行っても、減圧下で行ってもよい。水抽出の場合、最も問題になるのは糊化現象である。糊状になれば、抽出効率が悪くなるばかりでなく、実作業においては困難を極める。これを防ぐためには、アミラーゼを加えて反応させるか、塩酸などで酸性にして澱粉を切ってやればよく、この方法を用いることにより、十分に解決でき、実用上も全く問題はない。   When water is extracted from rice, a high extraction temperature is efficient, but extraction can be sufficiently performed even at a low temperature. However, in the case of a low temperature of 40 ° C. or lower, it is desirable that the pH is made acidic or alkaline, or a preservative or alcohol is added so that the rice is not spoiled. The extraction time may be long or short as long as the active ingredient can be extracted, and may be determined by the extraction temperature. The extraction may be performed under pressure, normal pressure, or reduced pressure. In the case of water extraction, the most serious problem is the gelatinization phenomenon. If it becomes paste-like, not only extraction efficiency will worsen but it will be extremely difficult in actual work. In order to prevent this, the reaction may be performed by adding amylase or acidifying with hydrochloric acid or the like to cut the starch. By using this method, the problem can be solved sufficiently and there is no problem in practical use.

抽出物中の有効成分は、酸,アルカリに安定であるためか、酸分解抽出、あるいはアルカリ分解抽出を行うのも有効である。この場合、必要により中和、脱塩を行う。有機溶媒で抽出する場合も、米はなるべく微粉砕または粉体化して抽出することが望ましい。有機溶媒はアルコール,アセトン,n―へキサン,メタノール等の一般的な有機溶媒でよいが、人体に対して有害なものは抽出後、溶媒を完全に除去する必要があるので安全なものがよい。また、米を酸素分解、または麹を作用させてもよい。ここで言う酸素分解とは、澱粉分解酵素(液化酵素、糖化酵素),蛋白分解酵素,脂肪分解酵素,繊維分解酵素,リグニン分解酵素,ペクチン分解酵素等米に働く酵素を1種または2種以上作用させることをいう。例えば、液化酵素と糖化酵素との組み合わせを挙げることができる。また、麹として麹菌の種類および米の品種,種類は問わない。   It is also effective to perform acid decomposition extraction or alkali decomposition extraction because the active ingredient in the extract is stable to acid and alkali. In this case, neutralization and desalting are performed as necessary. Also when extracting with an organic solvent, it is desirable to extract rice by pulverizing or pulverizing it as much as possible. The organic solvent may be a common organic solvent such as alcohol, acetone, n-hexane, methanol, etc., but those that are harmful to the human body should be safe because the solvent must be completely removed after extraction. . In addition, rice may be subjected to oxygen decomposition or rice bran. As used herein, oxygen degradation means one or more enzymes that act on rice, such as starch degrading enzymes (liquefaction enzymes, saccharifying enzymes), proteolytic enzymes, lipolytic enzymes, fiber degrading enzymes, lignin degrading enzymes, and pectin degrading enzymes. It means to act. For example, the combination of a liquefying enzyme and a saccharifying enzyme can be mentioned. In addition, the type of koji mold and the variety and type of rice are not questioned.

さらに、前記の抽出を行うに当り、抽出の前、抽出と同時または抽出の後に、上記の酵素分解および麹を作用させてもよい。本発明においては、さらに上記の処理を行なうと同時または処理後、アルコール発酵あるいは乳酸発酵、酢酸発酵等の有機酸発酵を行うと、次のような点でも有効である。アルコール発酵を行なえば、濃縮がしやすく、有効成分の濃縮が容易になる。なお、酵母による通気発酵、アルコール沈殿等を行なって除糖してもよい。   Furthermore, in performing the said extraction, you may make said enzyme decomposition | disassembly and soot act before extraction, simultaneous with extraction, or after extraction. In the present invention, when the above-described treatment is further performed, or when the organic acid fermentation such as alcohol fermentation, lactic acid fermentation, or acetic acid fermentation is performed simultaneously or after the treatment, the following points are also effective. When alcoholic fermentation is performed, concentration is easy and concentration of active ingredients becomes easy. Sugar may be removed by aeration fermentation with yeast, alcohol precipitation, or the like.

本発明に係る経口用老化防止剤を用いると、生命体の老化や細胞の老化が防止される。ここで、生命体とは、多細胞生物(ヒトを含む哺乳類といった高等動物も含む)をいう。また、細胞も、単細胞に限られず、複数の細胞から成り立つ、器官、臓器、組織、体液(血液やリンパ液のような液体)等も包含する概念である。また、「経口」とは、経皮(皮膚適用)以外の投与経路を意味する。経皮以外の投与経路とは、口投与、その他内服(経管、十二指腸内)である。皮膚は角質層で被われているため、経皮投与では成分が吸収されにくいが、これらの経路で投与されることにより、全身、局所を問わず目的とする作用部位へ有効成分を到達させ、効果を現すことができる。また、「老化防止」とは、老化防止、老化改善、若々しさ保持、若返りを意味し、例えば、生理機能の衰えを防止、改善すること、具体的な例示としては、生命体或いは個体、器官、臓器、組織、体液又は細胞の老化防止、老化改善、若々しさ保持、若返り、より具体的には、老化皮膚、老人性乾皮症、皮膚老化症状(しわ、ハリ・弾力の低下、たるみ、シミ、色の変化、乾燥)、記憶力低下、学習能力の低下、筋力の衰え、体力低下、内分泌系の機能の低下、視力の低下、聴力の低下、反射神経が鈍くなる、外からの刺激に対する反応が遅くなる、外からの刺激により起こった体の中の変化がもとの状態に戻るまでに時間がかかる、傷の治りが悪くなる、免疫機能の低下、ウイルス、細菌に対する抵抗力が衰える等の生理機能の低下に対する予防、改善効果を挙げることができる。さらには老化により発生する各種疾患に対し予防、改善効果をもつ。更に、真皮に対しても、体内から真皮に本発明に係る老化防止剤が直接働きかけ、真皮の老化防止効果を得ることができる。 When the oral antiaging agent according to the present invention is used, aging of living organisms and aging of cells are prevented. Here, the living organism refers to a multicellular organism (including higher animals such as mammals including humans). In addition, the cell is not limited to a single cell, but is also a concept including organs, organs, tissues, body fluids (fluids such as blood and lymph), and the like that are composed of a plurality of cells. In addition, “oral” means an administration route other than transdermal (skin application). The routes of administration other than transdermal, oral administration, and other oral (gavage, intraduodenal). Since the skin is covered with the stratum corneum, the component is difficult to be absorbed by transdermal administration, but by being administered by these routes, the active ingredient reaches the intended site of action regardless of the whole body or the local area, The effect can appear. The term “anti-aging” means prevention of aging, improvement of aging, maintenance of youthfulness, rejuvenation, for example, prevention and improvement of deterioration of physiological function, as a specific example, a living organism or an individual, Prevention of aging of organs, organs, tissues, body fluids or cells, improvement of aging, retention of youthfulness, rejuvenation, more specifically, aging skin, senile xerosis, skin aging symptoms (wrinkles, reduced elasticity, elasticity, Sagging, spots, color change, dryness), memory loss, learning ability decline, muscle weakness, physical strength decline, endocrine function decline, vision loss, hearing loss, reflexes become dull, external Slow response to stimuli, changes in the body caused by external stimuli take time to return to the original state, wound healing becomes poor, immune function declines, resistance to viruses and bacteria Against decline in physiological function Prevention, may be mentioned improvement. Furthermore, it has preventive and ameliorating effects on various diseases caused by aging. Furthermore, the anti-aging agent according to the present invention directly acts on the dermis from the body to the dermis, and the anti-aging effect of the dermis can be obtained.

以上のようにして得られた本発明品は、残渣を分離することなくそのまま、あるいは圧搾、濾過して用いる。そのまま用いるときは、殺菌あるいは除菌して製品にする。なお、本発明品は実際の用途に応じ、エアゾール剤、液剤、ゼリー剤、エリキシル剤、カプセル剤、顆粒剤、丸剤、懸濁剤、乳剤、散剤、細粒剤、錠剤、シロップ剤、注射剤、トローチ剤、リモナーデ剤等の剤型で用いることもできる。更には、食品や飲料に添加する処方もあり得る。なお、用途に応じて、他の配合成分や薬剤を添加してもよい。尚、本発明品の添加量は、添加対象となる医薬品、飲食品等の種類にもよるが、一般的に、製品100重量部当たり、本発明品エキスを0.0001〜90重量部、好適には0.01〜60重量部、最も好適には0.1〜30重量部添加する。また、本発明品の摂取量は、体重1kg当たり、一日0.0001〜100ml、好適には一日0.001〜50ml、最も好適には0.01〜20mlである。   The product of the present invention obtained as described above is used as it is, or after being squeezed and filtered without separating the residue. When it is used as it is, it is sterilized or sterilized to make a product. The product of the present invention is aerosol, liquid, jelly, elixir, capsule, granule, pill, suspension, emulsion, powder, fine granule, tablet, syrup, injection depending on the actual application. It can also be used in dosage forms such as agents, troches, and limonades. Furthermore, there may be a prescription added to foods and beverages. In addition, you may add another compounding component and a chemical | medical agent according to a use. In addition, although the addition amount of the product of the present invention depends on the kind of the drug to be added, food and drink, etc., generally 0.0001 to 90 parts by weight of the product extract of the present invention per 100 parts by weight of the product is preferable. Is added in an amount of 0.01 to 60 parts by weight, most preferably 0.1 to 30 parts by weight. The intake of the product of the present invention is 0.0001 to 100 ml per day, preferably 0.001 to 50 ml, most preferably 0.01 to 20 ml per kg body weight.

また、本発明にかかる経口用老化防止剤は様々な具体的用途に有用である。例えば、生命体或いは個体、器官、臓器、組織、細胞などの老化防止、老化改善、若々しさ保持、若返り;細胞活性、細胞周期、遺伝子の機能の老化防止、老化改善、若々しさ保持、若返り;循環器系(心臓、血管、血液・造血器系)、免疫系(リンパ性組織・器官、脾臓、胸腺)、皮膚、皮膚付属器官、消化器系(口唇、扁桃、歯、食道、胃、小腸、大腸、肝臓、胆管系、脾臓)、呼吸器系(鼻、咽頭、喉頭、器官、肺)、泌尿器系(腎臓、尿路)、性殖系(男性生殖器、女性生殖器)、内分泌系(下垂体、松果体、甲状腺、副腎)、脳、神経系(末梢神経、中枢神経)、代謝系(糖、脂質、尿酸代謝)、平衡・聴覚器、視覚器、各粘膜系、運動器(骨、関節、筋肉、腱、靱帯)などの老化防止、老化改善、若々しさ保持、若返りをあげることができる。尚、実際の製品との関係では、例えば、老化防止のために用いられるものである旨の表示を製品(例えば、薬剤、化粧品、飲食品)のパッケージ、パンフレット及び取扱説明書等に付した態様が好適である。このような表示を付することにより、本発明品がそのような効果を奏することが、ユーザに一目瞭然となる。ここで、「老化防止のために用いられるものである旨の表示」とは、老化防止を明記した場合のみならず、老化防止を示唆する表示も包含する。   The oral antiaging agent according to the present invention is useful for various specific uses. For example, prevention of aging of living organisms or individuals, organs, organs, tissues, cells, improvement of aging, retention of youthfulness, rejuvenation; prevention of aging of cell activity, cell cycle, gene function, improvement of aging, retention of youthfulness, Rejuvenation; cardiovascular system (heart, blood vessel, blood / hematopoietic system), immune system (lymphoid tissue / organ, spleen, thymus), skin, skin appendages, digestive system (lip, tonsils, teeth, esophagus, stomach) , Small intestine, large intestine, liver, bile duct system, spleen), respiratory system (nose, pharynx, larynx, organ, lung), urinary system (kidney, urinary tract), sex breeding system (male genital organ, female genital organ), endocrine system (Pituitary gland, pineal gland, thyroid gland, adrenal gland), brain, nervous system (peripheral nerve, central nervous system), metabolic system (sugar, lipid, uric acid metabolism), balance / hearing apparatus, visual instrument, each mucous system, motor organ (Bone, joints, muscles, tendons, ligaments) and other aging prevention, aging improvement, youthfulness, rejuvenation Door can be. In relation to the actual product, for example, an indication that it is used for preventing aging is attached to a package (for example, drug, cosmetics, food and drink), a brochure, an instruction manual, etc. Is preferred. By attaching such a display, it is obvious to the user that the product of the present invention has such an effect. Here, the “indication to be used for the prevention of aging” includes not only the case where the aging prevention is specified but also a display suggesting the aging prevention.

実施例1
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に液化酵素5gと水3Lを添加し、60℃で4時間放置した。その後、加熱昇温させ、冷却した後、濾過器を用いて固液分離を行い、ろ液2.5Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例2
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に麹250gと水3Lを添加し、55℃で16時間放置した。その後濾過器を用いて固液分離を行い、ろ液2.6Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例3
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に澱粉分解酵素5gと水3Lを添加し、55℃で16時間放置した。その後濾過器を用いて固液分離を行い、ろ液2.5Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例4
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に蛋白質分解酵素5gと水3Lを添加し、50℃で16時間放置した。その後濾過器を用いて固液分離を行い、ろ液2.3Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例5
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に繊維分解酵素5gと水3Lを添加し、50℃で16時間放置した。その後濾過器を用いて固液分離を行い、ろ液2.2Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例6
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に脂肪分解酵素5gと水3Lを添加し、50℃で16時間放置した。その後濾過器を用いて固液分離を行い、ろ液2.1Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例7
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に液化酵素5gと水3Lを添加し、60℃で4時間放置した。その後、加熱昇温させ、冷却した後、澱粉分解酵素5gを加え、55℃で4時間放置した。その後濾過器を用いて固液分離を行い、ろ液2.6Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例8
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に液化酵素5gと水3Lを添加し、60℃で4時間放置した。その後、加熱昇温させ、冷却した後、蛋白質分解酵素5gを加え、55℃で4時間放置した。その後濾過器を用いて固液分離を行い、ろ液2.5Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例9
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に液化酵素5gと水3Lを添加し、60℃で4時間放置した。その後、加熱昇温させ、冷却した後、脂肪分解酵素5gを加え、55℃で4時間放置した。その後濾過器を用いて固液分離を行い、ろ液2.5Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例10
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に液化酵素5gと水3Lを添加し、60℃で4時間放置した。その後、加熱昇温させ、冷却した後、繊維分解酵素5gを加え、55℃で4時間放置した。その後濾過器を用いて固液分離を行い、ろ液2.5Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例11
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に1/10N塩酸3Lを添加し、よく撹拌し24時間放置した。その後、濾過器を用いて固液分離を行い、苛性ソーダで中和し、2.3Lの抽出液を得た。これを85℃で30分加熱して本発明品を得た。
実施例12
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に95%エタノール3Lを添加し、よく撹拌し4日間放置した。その後、濾過器を用いて固液分離を行い、2Lの抽出液を得た。このろ液に水4Lを加え、ロータリーエバポレーターでエタノールを留去し2Lとした。これを85℃で30分加熱して本発明品を得た。
実施例13
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に液化酵素5gと水3Lを添加し、60℃で4時間放置した。その後、加熱昇温させ、冷却した後、澱粉分解酵素5gを加え、55℃で4時間放置した。その後冷却し酵母を加え、15日間発酵を行った。その後濾過器を用いて固液分離を行い、ろ液2.5Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例14
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に液化酵素5gと水3Lを添加し、60℃で4時間放置した。その後、加熱昇温させ、冷却した後、澱粉分解酵素5gを加え、55℃で4時間放置した。その後加熱殺菌し、冷却後乳酸菌を加え、37℃で2日間発酵を行った。その後濾過器を用いて固液分離を行い、ろ液2.3Lを得た。これを85℃で30分加熱して本発明品を得た。
実施例15
白米を粉砕機にかけ、白米の粉砕物1kgを得た。この粉砕物に液化酵素5gと水3Lを添加し、60℃で4時間放置した。その後、加熱昇温させ、冷却した後、澱粉分解酵素5gを加え、55℃で4時間放置した。その後95%エタノール150 mLと酢酸菌を加え、15日間発酵を行った。その後濾過器を用いて固液分離を行い、ろ液2.4Lを得た。これを85℃で30分加熱して本発明品を得た。
試験例1
個体は細胞により構成されていることから、細胞一つ一つの老化は、結果として個体の老化変化へとつながる。そこで、本発明品の老化防止効果を細胞レベルで検証した。
方法:コンフルエントに培養した小腸粘膜上皮細胞(IEC−6)に、1%試料を添加した培養液で30日間培養した。試料添加後、培地交換は行わなかった。
試料:実施例1〜実施例15。なお、実施例13は、ロータリーエバポレーターで減圧濃縮し、アルコール分を溜去した後、水を加え、もとの量に戻したものを試料として用いた。
結果:30日間培養した後のIEC−6を肉眼的に観察した結果、本発明品1%を添加した培地で培養した細胞では異常が全く認められず、正常な状態を維持し生存し続けていることが判明した。またその細胞は若々しかった。一方、本発明品を添加しなかった細胞では、生存し続けることができなかった。以上の試験から本発明品による老化防止、若々しさ保持効果が細胞レベルで証明された。
試験例2
試験例1により、本発明品の細胞に対する老化防止効果が証明された。そこで、次に実験動物を用いて個体全体の老化防止効果を調べた。
Example 1
The white rice was put into a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of liquefied enzyme and 3 L of water were added and left at 60 ° C. for 4 hours. Then, after heating up and cooling, solid-liquid separation was performed using the filter and 2.5 L of filtrate was obtained. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 2
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 250 g of candy and 3 L of water were added and left at 55 ° C. for 16 hours. Thereafter, solid-liquid separation was performed using a filter to obtain 2.6 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 3
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of starch-degrading enzyme and 3 L of water were added and left at 55 ° C. for 16 hours. Thereafter, solid-liquid separation was performed using a filter to obtain 2.5 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 4
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of proteolytic enzyme and 3 L of water were added and allowed to stand at 50 ° C. for 16 hours. Thereafter, solid-liquid separation was performed using a filter to obtain 2.3 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 5
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of a fiber-degrading enzyme and 3 L of water were added and left at 50 ° C. for 16 hours. Thereafter, solid-liquid separation was performed using a filter to obtain 2.2 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 6
The white rice was put into a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of lipolytic enzyme and 3 L of water were added and left at 50 ° C. for 16 hours. Thereafter, solid-liquid separation was performed using a filter to obtain 2.1 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 7
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of liquefied enzyme and 3 L of water were added and left at 60 ° C. for 4 hours. Thereafter, the temperature was raised by heating, and after cooling, 5 g of amylolytic enzyme was added and left at 55 ° C. for 4 hours. Thereafter, solid-liquid separation was performed using a filter to obtain 2.6 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 8
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of liquefied enzyme and 3 L of water were added and left at 60 ° C. for 4 hours. Then, after heating up and cooling, 5 g of proteolytic enzymes were added and left at 55 ° C. for 4 hours. Thereafter, solid-liquid separation was performed using a filter to obtain 2.5 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 9
The white rice was put into a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of liquefied enzyme and 3 L of water were added and left at 60 ° C. for 4 hours. Thereafter, the temperature was raised by heating, and after cooling, 5 g of lipolytic enzyme was added and left at 55 ° C. for 4 hours. Thereafter, solid-liquid separation was performed using a filter to obtain 2.5 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 10
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of liquefied enzyme and 3 L of water were added and left at 60 ° C. for 4 hours. Then, after heating up and cooling, 5 g of fiber-degrading enzymes were added and left at 55 ° C. for 4 hours. Thereafter, solid-liquid separation was performed using a filter to obtain 2.5 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 11
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 3 L of 1 / 10N hydrochloric acid was added, stirred well and allowed to stand for 24 hours. Thereafter, solid-liquid separation was performed using a filter and neutralized with caustic soda to obtain 2.3 L of an extract. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 12
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 3 L of 95% ethanol was added, stirred well and left for 4 days. Thereafter, solid-liquid separation was performed using a filter to obtain a 2 L extract. 4 L of water was added to the filtrate, and ethanol was distilled off with a rotary evaporator to 2 L. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 13
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of liquefied enzyme and 3 L of water were added and left at 60 ° C. for 4 hours. Thereafter, the temperature was raised by heating, and after cooling, 5 g of amylolytic enzyme was added and left at 55 ° C. for 4 hours. After cooling, yeast was added and fermentation was performed for 15 days. Thereafter, solid-liquid separation was performed using a filter to obtain 2.5 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 14
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of liquefied enzyme and 3 L of water were added and left at 60 ° C. for 4 hours. Thereafter, the temperature was raised by heating, and after cooling, 5 g of amylolytic enzyme was added and left at 55 ° C. for 4 hours. Thereafter, the mixture was sterilized by heating, cooled, added with lactic acid bacteria, and fermented at 37 ° C. for 2 days. Thereafter, solid-liquid separation was performed using a filter to obtain 2.3 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Example 15
White rice was ground in a grinder to obtain 1 kg of white rice grind. To this pulverized product, 5 g of liquefied enzyme and 3 L of water were added and left at 60 ° C. for 4 hours. Thereafter, the temperature was raised by heating, and after cooling, 5 g of amylolytic enzyme was added and left at 55 ° C. for 4 hours. Thereafter, 150 mL of 95% ethanol and acetic acid bacteria were added, and fermentation was performed for 15 days. Thereafter, solid-liquid separation was performed using a filter to obtain 2.4 L of a filtrate. This was heated at 85 ° C. for 30 minutes to obtain the product of the present invention.
Test example 1
Since an individual is composed of cells, aging of each cell results in aging changes of the individual. Therefore, the anti-aging effect of the product of the present invention was verified at the cell level.
Method: Intestinal mucosal epithelial cells (IEC-6) cultured confluently were cultured in a culture medium supplemented with a 1% sample for 30 days. The medium was not changed after the sample was added.
Sample: Example 1 to Example 15. In Example 13, the sample was concentrated under reduced pressure using a rotary evaporator, the alcohol content was distilled off, water was added, and the amount returned to the original amount was used as a sample.
Results: As a result of macroscopic observation of IEC-6 after 30 days of culture, no abnormalities were observed in cells cultured in a medium supplemented with 1% of the product of the present invention, and the cells remained normal and continued to survive. Turned out to be. The cells were young. On the other hand, the cells to which the product of the present invention was not added could not continue to survive. From the above tests, the effects of the present invention on preventing aging and maintaining youthfulness were proved at the cellular level.
Test example 2
Test Example 1 proved the anti-aging effect of the product of the present invention on cells. Then, the anti-aging effect of the whole individual | organism | solid was investigated using the experimental animal next.

一般に、動物から発生する熱の変化を測定することで、体の状態の変化を知ることが出来る。流出熱量には1日のリズム(日内リズム)があり、夜行性のマウスは、夜は流出量が多く昼間は少ない。夜と昼の流出熱量差が大きく日内変動がはっきりしているほど若々しいとされ、このリズムの平坦化(夜昼差がゼロ付近になること)は、個体全体の老化の指標となる。また、総熱量も老化とともに減少する。そこで、老化現象が早く進むことが知られているSAMマウスを用いて、熱量の変化及び一般状態の変化を指標とし、本発明品の老化防止効果を調べた。   In general, changes in the state of the body can be known by measuring changes in heat generated from animals. There is a daily rhythm in the amount of heat released (nocturnal rhythm), and nocturnal mice have a large amount of outflow at night and a small amount during the day. It is said that the difference in calorific value between night and day is large and the fluctuation in the daytime is clear. The level of this rhythm (the night-day difference being near zero) is an indicator of aging of the whole individual. In addition, the total amount of heat decreases with aging. Therefore, using an SAM mouse that is known to accelerate the aging phenomenon, the effect of preventing the aging of the product of the present invention was examined using changes in calorific value and changes in the general state as indices.

使用した動物SAMマウスは、遺伝的に短命という特徴をもつ系統であり、成体になるまでの期間は通常のマウスと変わりないが、皮膚のつやの消失、皮膚の荒れの増加、体毛の消失、免疫機能の低下、聴覚機能の低下、脳の萎縮などの老化現象が早く進むこと、加齢に伴い、学習能力や記憶力が低下することが知られている。特に26週から35週の間で老化が明らかに現れるとされているため、15週齢から35週齢の期間に測定と観察を行った。
方法:9週齢の雄性SAMマウス5匹を通常の食餌、飲水を自由にさせた状態で6週間予備飼育した。5匹中3匹は、予備飼育後本発明品を含む餌を与え35週齢まで飼育した。残りの2匹は、通常の餌を与え35週齢まで飼育した。15週齢から35週齢までの期間に熱量計を用いたマウス熱量の測定、一般状態の肉眼的観察を行った。熱量計の中には、充分な水と餌を用意し、運動できるよう回転輪を設置し、また昼と夜の区別がつくように窓を設けた。
試料:実施例14
結果:長期飼育試験の結果、本発明品配合の餌を与えたSAMマウス(本発明品群)は、15週齢〜35週齢のいずれの時期においても、夜と昼の流出熱量差が大きく日内変動がはっきりしており、老化の指標となる日内リズムの平坦化は認められなかった(図1)。なお、投与前の15週齢と比較して、投与後の19週齢〜35週齢の方がより一層日内変動がはっきりしてきた。また、一日の総熱量も徐々に上昇し(図2)、通常の餌を与えたSAMマウス(コントロール群)と比較しても顕著に高かった。一方コントロール群は、23週齢〜35週齢で日内リズムの平坦化が顕著に認められ、一日の総熱量も経時的に低下していった。これより、本発明品は個体全体の老化を防止、改善し、若々しさ保持、若返り効果をもつことが判明した。
The animal SAM mice used are genetically short-lived strains, and the period until adulthood is the same as that of normal mice, but loss of skin gloss, increased skin roughness, loss of hair, immunity It is known that aging phenomena such as functional decline, auditory function decline, and brain atrophy progress rapidly, and that learning ability and memory ability decline with aging. In particular, since it is said that aging clearly appears between 26 and 35 weeks, measurements and observations were made during the period of 15 to 35 weeks of age.
Method: Five 9-week-old male SAM mice were preliminarily raised for 6 weeks in a state in which normal food and drinking water were freely available. Three of the five animals were fed up to 35 weeks of age after receiving a food containing the product of the present invention after preliminary breeding. The remaining two were fed normal food and were raised to 35 weeks of age. During the period from 15 weeks of age to 35 weeks of age, the calorific value of the mouse was measured using a calorimeter, and the general state was observed visually. In the calorimeter, enough water and food were prepared, a rotating wheel was set up to exercise, and a window was provided to distinguish day and night.
Sample: Example 14
Results: As a result of the long-term breeding test, the SAM mice (invention group) fed with the diet of the present invention have a large difference in the calorific value between night and day at any time from 15 to 35 weeks of age. The circadian variation was clear and the circadian rhythm, which is an index of aging, was not flattened (Fig. 1). In addition, compared with the 15-week-old before administration, the diurnal variation became clearer at 19-35 weeks after administration. Moreover, the total amount of heat per day also gradually increased (FIG. 2), and was significantly higher than that of the SAM mice (control group) fed with normal food. On the other hand, in the control group, the flattening of the daily rhythm was remarkably observed at 23 to 35 weeks of age, and the total heat amount of the day also decreased with time. From this, it was found that the product of the present invention has the effect of preventing and improving the aging of the whole individual and maintaining the youthfulness and rejuvenation.

一般状態を観察したところ、28週齢頃からコントロール群は熱量計に入れると必ず尾に怪我をした。回転輪を回すときに尾を金網に挟まれてしまうのが原因の一つであったが、これは老化による運動能力や反射神経の低下、視力の低下、ボケのためと考えられた。一方、本発明品群では、尾の怪我も見られず、回転輪での運動の様子から運動能力、反射神経、視力の低下、ボケなどの老化変化は認められなかった。   When the general state was observed, the control group was injured in the tail whenever it was put into the calorimeter from the age of 28 weeks. One of the causes was that the tail was pinched by the wire mesh when turning the rotating wheel, but this was thought to be due to the deterioration of motor ability, reflexes, visual acuity, and blur due to aging. On the other hand, in the product group of the present invention, no tail injury was observed, and no changes in aging such as motor ability, reflexes, visual acuity, and blur were observed from the state of motion on the rotating wheel.

また35週齢になるとコントロール群では、皮膚につやが無く、荒れており、体毛も薄くなっていたが、本発明品群は皮膚、体毛の老化変化は認められなかった。   Further, at the age of 35 weeks, in the control group, the skin was not glossy, rough, and the hair was thin, but in the product group of the present invention, no change in aging of the skin and hair was observed.

以上の通り、個体全体の老化の指標である熱量の日内リズム、総熱量の変化から、本発明品は体全体の老化を防止することが証明された。また観察の結果、皮膚や毛の老化変化、運動能力や反射神経、視力の低下、ボケ等の老化変化を防ぐことが認められた。さらに本発明品は、SAMマウスの老化の特徴である免疫機能、聴覚機能の低下、脳の萎縮、学習能力、記憶能力の低下などを防止しているものと考えられた。   As described above, it was proved that the product of the present invention prevents the aging of the whole body from the daily rhythm of the calorific value and the change of the total calorific value, which are indicators of aging of the whole individual. As a result of observation, it was confirmed that aging changes of skin and hair, motor ability and reflexes, deterioration of visual acuity, and aging changes such as blur were prevented. Furthermore, it was considered that the product of the present invention prevents immunity, auditory function, brain atrophy, learning ability, and memory ability, which are characteristic of aging in SAM mice.

また本発明品は個体全体の老化を防止、改善し、若々しさ保持、若返り効果をもつことから、試験例1で証明した細胞の老化防止、若返り効果は、試験に使用した小腸粘膜上皮細胞だけでなく、他の細胞でも同様の効果を現すことがわかった。   Further, since the product of the present invention has the effect of preventing and improving the aging of the whole individual and maintaining the youthfulness and the rejuvenation effect, the anti-aging and rejuvenation effect of the cells proved in Test Example 1 is the same as the intestinal mucosal epithelial cells used in the test. It was found that the same effect was exhibited not only in other cells.

試験例1〜2より、本発明品には個体、器官、臓器、組織、細胞などの老化防止、改善、若さ保持、若返り効果、遺伝子の機能の老化防止、老化改善、若々しさ保持、若返り効果をもつことが明らかとなった。   From Test Examples 1 and 2, the product of the present invention has aging prevention, improvement, rejuvenation retention, rejuvenation effect of individuals, organs, organs, tissues, cells, etc., aging prevention of gene function, aging improvement, youthfulness retention, It became clear that it had a rejuvenating effect.

図1は、試験例2に従い、本発明(実施例14)に係る老化防止効果がマウス日内リズムにどの程度影響を及ぼすか調べたものである。FIG. 1 is an examination of how much the anti-aging effect according to the present invention (Example 14) affects the circadian rhythm according to Test Example 2. 図2は、試験例2に従い、本発明(実施例14)に係る老化防止効果がマウス総熱量にどの程度影響を及ぼすか調べたものである。FIG. 2 is a graph showing how the anti-aging effect according to the present invention (Example 14) affects the total amount of heat in mice according to Test Example 2.

Claims (1)

白米粉砕物を液化酵素及び糖化酵素で順次処理した後、乳酸発酵を行ったものを有効成分として含有する、日内リズムの平坦化抑制及び一日の総熱量低下防止のための経口用老化防止剤。 Oral anti-aging agent for suppressing flattening of circadian rhythm and preventing a decrease in the total calorific value of the day, containing as an active ingredient the processed pulverized white rice with liquefaction enzyme and saccharification enzyme, followed by lactic acid fermentation .
JP2004066262A 2004-03-09 2004-03-09 Anti-aging agent for oral use Expired - Lifetime JP5296957B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2004066262A JP5296957B2 (en) 2004-03-09 2004-03-09 Anti-aging agent for oral use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2004066262A JP5296957B2 (en) 2004-03-09 2004-03-09 Anti-aging agent for oral use

Publications (2)

Publication Number Publication Date
JP2005255557A JP2005255557A (en) 2005-09-22
JP5296957B2 true JP5296957B2 (en) 2013-09-25

Family

ID=35081648

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004066262A Expired - Lifetime JP5296957B2 (en) 2004-03-09 2004-03-09 Anti-aging agent for oral use

Country Status (1)

Country Link
JP (1) JP5296957B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106309278B (en) * 2016-08-31 2020-05-08 澳宝化妆品(惠州)有限公司 Agave fermentation product for anti-aging cosmetics and preparation method and application thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01316328A (en) * 1988-06-15 1989-12-21 Mitsui Toatsu Chem Inc Drug for preventing aging, activating cell and preventing and treating senile disease
JPH0741426A (en) * 1993-05-25 1995-02-10 Soken Kk Active oxygen scavenger from rice
JPH07165595A (en) * 1993-12-15 1995-06-27 Soken Kk Lipid metabolism improver prepared from rice
JP3568891B2 (en) * 1999-10-14 2004-09-22 日清オイリオ株式会社 Food and drink containing olive extract

Also Published As

Publication number Publication date
JP2005255557A (en) 2005-09-22

Similar Documents

Publication Publication Date Title
ES2599830T3 (en) Fermentation and cultivation method, fermented vegetable extract, fermented vegetable extract powder and composition containing fermented vegetable extract
CN104982928B (en) A kind of japanese yew fruit health care ferment and preparation method thereof
CN106794202A (en) Improve the composition and method of human health and nutrition
TWI516280B (en) Use of chenopodium formosanum extract for manufacture of composition for enhancing secretion of collagen and preventing cutaneous aging
JP2024052922A (en) Composition containing lactic acid bacteria production substance, method for producing equol, and method for producing composition containing lactic acid bacteria production substance
CN106962933B (en) Application of nymphaea hybrid extract and composition thereof in preventing obesity and improving intestinal flora
CN107057917A (en) Hydromel and preparation method thereof
KR101866636B1 (en) Composition for blood circulation comprising fermented ginger and mature ginger
CN109259022A (en) A kind of drink containing small-molecular peptides that can quickly improve microcirculation function
CN108186542A (en) Lip care lipstick with antiallergic effect of releiving
CN112057491A (en) Application of copperleaf herb water extract in preparation of weight-losing and lipid-lowering medicines or weight-losing and lipid-lowering health-care products
CN115154393B (en) Aloe fermentation liquor and preparation method and application thereof
JP5296957B2 (en) Anti-aging agent for oral use
CN106659752A (en) Composition containing scutellaria alpina extract
JP5307969B2 (en) Life extension agent containing white rice-derived ingredients as active ingredients
JP5514390B2 (en) Life extension agent made from cereals and beans other than rice
CN106176510A (en) A kind of oral thing for aesthetic health care and corresponding beautifying health composition
CN104837336B (en) Saltant type tomato and its purposes for preventing increased weight and/or treatment obesity-related disease
JP4772354B2 (en) Life extension agent made from rice
CN109620858A (en) The integration of drinking and medicinal herbs preparation for preventing and treating diabetes
CN109497228A (en) A kind of brown sugar ginger tea and preparation method thereof
JP2015221760A (en) Collagen synthetic promoter, hyaluronic acid synthetic promoter, and ceramide synthetic promoter
Oguntoye et al. Provitamin A cassava hydrolysate with Lactobacillus rhamnosus GG regulates weight gain, lipids and postprandial glycemia in wistar rats and humans
JP3779740B2 (en) Agents for preventing and treating obesity from rice
CN110740741A (en) Processed product of purslane, method for producing processed product of purslane, supplement, pharmaceutical, intestinal mucosa protective agent, and intestinal conditioning agent

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20070130

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100506

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100705

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20100817

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20130417

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20130614

R150 Certificate of patent or registration of utility model

Ref document number: 5296957

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

EXPY Cancellation because of completion of term